- Trials with a EudraCT protocol (1,915)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (36)
1,915 result(s) found for: Renal failure.
Displaying page 1 of 96.
EudraCT Number: 2010-022994-32 | Sponsor Protocol Number: 34009 | Start Date*: 2011-06-24 | ||||||||||||||||
Sponsor Name:UMC Utrecht | ||||||||||||||||||
Full Title: Effect of N-acetylcysteine on hydrogen sulfide in chronic kidney disease | ||||||||||||||||||
Medical condition: Chronic kidney disease End stage renal disease | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-008246-20 | Sponsor Protocol Number: ABR 25995 | Start Date*: Information not available in EudraCT | |||||||||||||||||||||
Sponsor Name:Radboud University Nijmegen Medical Center, Department of Anaesthesiology, Pain and Palliative Medic | |||||||||||||||||||||||
Full Title: Evaluation of the efficacy and safety of sugammadex (Bridion) in children with renal failure. | |||||||||||||||||||||||
Medical condition: Sugammadex is a selective relaxant binding agent, which is administered in case of a rocuronium-induced neuromuscular block, during general anaesthesia. The aim of the trial is to investigate the u... | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001296-32 | Sponsor Protocol Number: FC/HULP-2014_01 | Start Date*: 2014-07-07 | ||||||||||||||||
Sponsor Name:Fundación para la Investigación Biomédica del Hospital Universitario de La Paz | ||||||||||||||||||
Full Title: Pharmacokinetic and pharmacodynamic optimization of amikacin treatment in patients with terminal renal failure under conventional hemodialysis: randomized clinical trial of two model of administration | ||||||||||||||||||
Medical condition: Terminal renal failure under hemodialysis | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002267-25 | Sponsor Protocol Number: PIVOTAL | Start Date*: 2013-09-06 | ||||||||||||||||||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust | ||||||||||||||||||||||||||||
Full Title: UK Multicentre Open-label Randomised Controlled Trial Of IV Iron Therapy In Incident Haemodialysis Patients | ||||||||||||||||||||||||||||
Medical condition: Iron-deficiency in anaemia of end stage renal disease. | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-000894-94 | Sponsor Protocol Number: KOR-PED-201 | Start Date*: 2021-08-26 | ||||||||||||||||
Sponsor Name:Vifor Fresenius Medical Care Renal Pharma Ltd. | ||||||||||||||||||
Full Title: An Open-label, Single Arm Study to Evaluate the Pharmacokinetics of a Single Dose of Intravenous Difelikefalin in Adolescents Aged 12 to 17 Years on Haemodialysis | ||||||||||||||||||
Medical condition: Renal disease in the final stage | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-018838-45 | Sponsor Protocol Number: RLY5016–204 | Start Date*: 2010-04-21 | ||||||||||||||||
Sponsor Name:Relypsa, Inc. | ||||||||||||||||||
Full Title: A Multicenter, Open-Label, Single-Arm Study to Evaluate a Titration Regimen for RLY5016 in Heart Failure Patients with Chronic Kidney Disease | ||||||||||||||||||
Medical condition: Heart failure with Chronic kidney disease | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SI (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-002586-38 | Sponsor Protocol Number: RPH-1101 | Start Date*: 2011-10-14 | |||||||||||
Sponsor Name:Renapharma AB | |||||||||||||
Full Title: A 12-week clinical double-blind, randomised study of cholecalciferol versus placebo in patients with chronic kidney disease stage 3-4 (CHICK). | |||||||||||||
Medical condition: Chronic renal failure, stage 3-4 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005003-88 | Sponsor Protocol Number: SIM15 | Start Date*: 2016-03-15 | |||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and University of Cambridge | |||||||||||||
Full Title: Survival Improvement with Cholecalciferol in Patients on Dialysis – The SIMPLIFIED Registry Trial | |||||||||||||
Medical condition: Kidney Failure (requiring dialysis). | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002744-24 | Sponsor Protocol Number: 1058/12 | Start Date*: 2012-12-16 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Effect of oral paricalcitol on endothelial function and FGF-23 in peritoneal dialysis patients: a pilot study | |||||||||||||
Medical condition: CHRONIC RENAL FAILURE | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003081-32 | Sponsor Protocol Number: 1160.166 | Start Date*: 2012-04-18 | ||||||||||||||||
Sponsor Name:Boehringer Ingelheim bv | ||||||||||||||||||
Full Title: An exploratory study to investigate the pharmacokinetics and effects of DABIgatran etexilate in patients with stable severe RENAL disease: DabiRenal | ||||||||||||||||||
Medical condition: Chronic kidney disease and coagulation | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-006168-30 | Sponsor Protocol Number: RLH_Pentoxifylline_Dec2011 | Start Date*: 2013-01-08 | |||||||||||
Sponsor Name:R&D, Barts and The London NHS Trust | |||||||||||||
Full Title: PEntoxifylline in Anaemia Resistant to erythropoietin (PEAR) | |||||||||||||
Medical condition: We shall study patients with renal failure on dialysis. We shall particularly focus on patients with evidence of erythopoeitin stimulating agent (ESA) resistance. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020114-29 | Sponsor Protocol Number: IGFHD1-2010 | Start Date*: 2010-07-13 | |||||||||||
Sponsor Name:Department of Nephrology | |||||||||||||
Full Title: Insulin-like growth factor in hemodialysis patients | |||||||||||||
Medical condition: This project aims to investigate whether the anabolic potentials of insulin may be used to reverse the catabolic effects of hemodialysis in non-diabetic patients with end-stage renal failure. Thus... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000856-16 | Sponsor Protocol Number: DTG_HD | Start Date*: 2015-05-27 | ||||||||||||||||
Sponsor Name:Fundació Lluita contra la SIDA | ||||||||||||||||||
Full Title: Removal of dolutegravir by hemodialysis in HIV-infected patients with end-stage renal disease. | ||||||||||||||||||
Medical condition: HIV-infected patients with end-stage renal disease | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-000740-29 | Sponsor Protocol Number: 270389-030122 | Start Date*: 2022-04-12 | ||||||||||||||||
Sponsor Name:Department of Renal Medicine, Aarhus University Hospital | ||||||||||||||||||
Full Title: Sodium glucose cotransporter 2 inhibitors or Mineralocorticoid receptor antagonists for the treatment of Albuminuric Chronic Kidney Disease - A randomized controlled trial | ||||||||||||||||||
Medical condition: Chronic Kidney Disease with albuminuria | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-001200-23 | Sponsor Protocol Number: CCFM 103/208 | Start Date*: 2008-07-13 | |||||||||||
Sponsor Name:FONDAZIONE MONZINO CENTRO CARDIOLOGICO | |||||||||||||
Full Title: A Study to Evaluate the Effectiveness of Induced Diuresis with Matched Hydration Therapy Compared to Standard Overnight Hydration in the Prevention of Contrast Induced Nephropathy | |||||||||||||
Medical condition: Patients with moderate to severe renal failure candidates to angiographic procedures at high risk for CIN | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001407-11 | Sponsor Protocol Number: Certican MHH PRTx01 | Start Date*: 2006-07-18 | |||||||||||
Sponsor Name:Medizinische Hochschule Hannover | |||||||||||||
Full Title: A single center study investigating ciclosporine A microemulsion in combination with basiliximab and prednisolon and switch to low-dose ciclosporine A and everolimus without steroids in the prevent... | |||||||||||||
Medical condition: Kidney transplantation after end stage renal failure | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000948-98 | Sponsor Protocol Number: H-3-2011-154 | Start Date*: 2012-05-03 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: Effect of epinephrine on systemic absorption of mepivacaine administered for brachial plexus block in patients with end-stage renal disease | |||||||||||||
Medical condition: End-stage renal disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003496-29 | Sponsor Protocol Number: I13034 | Start Date*: 2014-10-24 | |||||||||||
Sponsor Name:University Hospital, Limoges | |||||||||||||
Full Title: Designing a Bayesian model of the plasma clearance of Calcium edetate de sodium, with a limited sampling strategy for the calculation of Glomerular Filtration Rate (GFR) and validity assessment com... | |||||||||||||
Medical condition: Chronic Kidney Disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006014-20 | Sponsor Protocol Number: FARM6X822T | Start Date*: 2009-01-19 | |||||||||||
Sponsor Name:CONSORZIO MARIO NEGRI SUD | |||||||||||||
Full Title: Effects of the dose of erythropoiesis stimulating agents on cardiac-cerebrovascular outcomes and quality of life in hemodialysis patients. The DOSe of Erythropoietins (DOSE) trial. | |||||||||||||
Medical condition: End stage kidney disease and anemia, treated with hemodialysis for renal replacement therapy | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016362-85 | Sponsor Protocol Number: ST1472-DM-09-005 | Start Date*: 2009-11-09 | |||||||||||
Sponsor Name:SIGMA-TAU | |||||||||||||
Full Title: A PILOT, RANDOMIZED, SINGLE SITE, 3 PARALLEL ARMS, OPEN-LABEL STUDY IN PATIENTS ON CHRONIC DIALYSIS WITH END STAGE RENAL DISEASE (ESRD) TO EVALUATE THE ENHANCING EFFECT OF TWO DOSES OF THYMOSIN ALP... | |||||||||||||
Medical condition: ZADAXIN ENHANCING EFFECT IN PATIENTS ON CHRONIC DIALYSIS WITH END STAGE RENAL DISEASE (ESRD) TREATED WITH EGG-DERIVED H1N1sw MONOVALENT INFLUENZA VACCINE | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
